Matthias Steib
Technische Universität München
6 Papers
25 Citations
Matthias Steib is an academic researcher from Technische Universität München. The author has contributed to research in topics: Adsorption & Catalysis. The author has an hindex of 6, co-authored 6 publications. Previous affiliations of Matthias Steib include Paul Scherrer Institute.
Chat about Author
Papers
Mechanism and Kinetics of CO2 Adsorption on Surface Bonded Amines
TL;DR: The impact of H2O on the mechanism and kinetics of CO2 adsorption by amine-impregnated SBA-15 has been investigated in this paper.
131
Design of stable Ni/ZrO2 catalysts for dry reforming of methane
Yu Lou,Matthias Steib,Qi Zhang,Qi Zhang,Konrad Tiefenbacher,Konrad Tiefenbacher,Anita Horváth,Andreas Jentys,Yue Liu,Johannes A. Lercher +9 more
TL;DR: The Ni/ZrO2 catalyst with a 1.1"nm particle diameter showed outstanding stability in dry reforming of methane (DRM), which maintained nearly 90% of the initial activity after 60'h time on stream as mentioned in this paper.
102
Enhanced Activity in Methane Dry Reforming by Carbon Dioxide Induced Metal-Oxide Interface Restructuring of Nickel/Zirconia
TL;DR: In this paper, Ni/ZrO2 catalysts for dry reforming of methane are significantly enhanced by activation and regeneration in presence of CO2 and exposure to CO2 maximizes and dynamically restructures the Ni-ZRO2 interface, which is critical for obtaining stable catalysts.
28
On‐Stream Regeneration of a Sulfur‐Poisoned Ruthenium–Carbon Catalyst Under Hydrothermal Gasification Conditions
TL;DR: In this paper, a method to remove S from a S-poisoned Ru catalyst under hydrothermal conditions through an oxidative treatment in the aqueous phase was developed, which led to a significant increase in carbon-to-gas conversion and methane selectivity.
15
Tailoring hierarchically structured SiO2 spheres for high pressure CO2 adsorption
TL;DR: In this paper, the synthesis, characterization, and experimental validation of hierarchically structured, millimeter-sized SiO2 spheres with high CO2 uptake capacities have been systematically explored, and the new sorbents possess specific surface areas up to 660 m2 g−1 and a hierarchically ordered mesoporous/macroporous pore structure.
15